Skip to main content
OpenTrials
Completed

NCT Number: NCT01692067

Deployment Health in Regular Military Women

The purpose of this study is to determine potential risk factors for physical and sexual assault in regular military women (as opposed to Reserve and National Guard). In addition, this study seeks to determine associations between service women's violence exposures and: current physical and mental health status (e.g. PTSD), and access to and use of DoD, DVA and civilian healthcare.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Anne G. Sadler, Ph.D.; VAMC, Iowa City, Iowa, United States

Loading trial locations.

About this study

Background: The proposed study of Regular Military service women builds on and extends a funded VA HSR&D grant currently investigating similar objectives in Reserves and National Guard (R/NG) service women. This proposed study addresses the radically changing DoD and DVA health care delivery needs of two priority populations: women exposed to combat, and women sexually assaulted during military. There is a limited understanding of the complex relationship between these traumatic exposures and women's health outcomes, such as post-traumatic stress disorder (PTSD) and traumatic brain injury (TBI) and with their subsequent health service use or barriers to care.

Objectives: The objectives are: 1) To identify and describe organizational, situational, and individual risk factors for physical and sexual assault (i.e., victimization) in women who have served or are currently serving in the Regular Military in Operation Enduring Freedom and Operation Iraqi Freedom (OEF/OIF) by deployment status (those who are deployed to combat related regions once, those deployed more than once, those serving in non-combat related areas outside of the continental United States (US), or those serving within the continental US. 2) To determine associations between PTSD, TBI, and physical and sexual assault during OEF/OIF with current physical and mental health status and health risk behaviors by deployment status. 3) To identify current internal and external barriers to DoD, DVA, and civilian health services in relationship to women's deployment and victimization status and the association between PTSD and TBI; 4) To identify and describe differences between Regular Military and R/NG populations for each of these objectives.

Methods: We propose a cross sectional study design with two sequential phases. Phase 1 would include focus groups to refine the current study interview specific to Regular Military populations. Phase 2 would involve the identification and successful interviewing of 669 Regular Military service women, using random sampling with stratification by deployment status, state of service accession, and service branch. Building on our current study, women will be selected from five states: Iowa, Illinois, Kansas, Missouri, and Nebraska. Potential study participants will be mailed an information summary and asked to take part in a study assessing the deployment health of military women. 1058 women will be contacted to obtain the target of 669 completed interviews. Consenting participants (167 per deployment group) will complete a telephone interview that assesses socio-demographic variables, trauma exposures, health history, current health status, military environmental factors (organizational and situational factors), military and DVA health care and barriers to this care, and self reported service use. Descriptive analysis and multiple logistic regression analysis will be used.

Implications: It is unclear if the needs of military women are met by current combat-associated PTSD treatments originally based on male populations. It is anticipated that our findings will improve understanding of the health risks and outcomes of deployed Regular Military service women in contrast to women serving in the R/NG (with PTSD and TBI as key outcome variables). Our results consequently will have implications for DoD and DVA evidence based interventions for both primary prevention and care.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Focus Group:
  • Men or women who have or are currently active duty regular military (RM) of OIF/OEF service eras (10/7/01- present)
  • Interview phase:
  • Women, who have or are currently serving active duty RM during OIF/OEF service eras

Exclusion criteria

  • Focus Group:
  • Disabilities that render incapable of hearing
  • Comprehending
  • Communicating in a group or inhibit travel to focus group
  • Interview phase:
  • Disabilities that render incapable of hearing
  • Comprehending
  • Communicating independently with interviewers by telephone
  • Not having telephone and unable to access a nearby VA or other possible resource to contact toll free number.

Treatment and study plan

Primary outcomes

  1. Organizational, situational, and individual risk factors for physical and sexual assault in women who have or currently serving in active duty Regular Military in OIF/OEF by deployment status.

    Time frame: Months 28-42 of grant

Secondary outcomes

  1. Traumatic brain injury

    Time frame: Months 28-42 of grant

  2. Current internal (e.g. PTSD) and external barriers (e.g. access to care factors)to health services

    Time frame: Months 28-42 of grant

  3. Identification and description of differences between Regular Military and Reserve/National Guard service women for each of these aims (building on currently funded grant).

    Time frame: Months 28-42 of grant

  4. PTSD

    Time frame: Months 28-42 of Grant

  5. Current medical health, including reproductive health

    Time frame: Months 28-42 of grant

  6. Deployment factors associated with risk of violence/health

    Time frame: Months 28-42 of grant

Sponsors and collaborators

Lead sponsor

Iowa City Veterans Affairs Medical Center

Fed

Collaborators

  • US Department of Veterans Affairs
  • United States Department of Defense

Registry information

Official study title

Combat, Sexual Assault and Post-Traumatic Stress in OIF/OEF Military Women

Acronym: DHRMS

Important dates

Study start
2009
Primary completion
2013
Study completion
2013
First posted
Sep 25, 2012
Registry last updated
Jul 19, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.